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Showing 331 - 345 of 582 results
  • Chute CG, Ullman-Cullere M, Wood G, Lin S, He M, Pathak J. (2013 October). Some experiences and opportunities for big data in translational research. GENETICS IN MEDICINE. 15(10):802-809.
    PubMed ID: 24008998
  • Hartzler A, McCarty CA, Rasmussen LV, Williams M, Brilliant MH, Bowton E,...Trinidad S. (2013 October). Stakeholder engagement: a key component of integrating genomic information into electronic health records. GENETICS IN MEDICINE. 15(10):792-801.
    PubMed ID: 24030437
  • Kho A, Rasmussen LV, Connolly J, Peissig PL, Starren J, Hakonarson H, Hayes M. (2013 October). Practical challenges in integrating genomic data into the electronic health record. GENETICS IN MEDICINE. 15(10):772-8.
    PubMed ID: 24071798
  • Ji Y, Biernacka JM, Hebbring S, Chai Y, Jenkins GD, Batzler A,...Mrazek DA. (2013 October). Pharmacogenomics of selective serotonin reuptake inhibitor treatment for major depressive disorder: genome-wide associations and functional genomics. Pharmacogenomics J.. 13(5):456-63.
    PubMed ID: 22907730
  • Kimmel SE, French B, Anderson JL, Gage BF, Johnson JA, Rosenberg Y,...Ellenberg J [including Caldwell MD.] (2013 September). Rationale and design of the Clarification of Optimal Anticoagulation through Genetics trial. AMERICAN HEART JOURNAL. 166(3):435-41.
    PubMed ID: 24016491
  • Zhou Z, He M, Brilliant M, Brautbar A, Miller A, Weichelt B, Lin S. (2013 September). PS3-2: Informatics Challenges to Implement Pharmacogenetics to Clinical Practice. Clin Med Res. 11(3):147-148.
  • Margolis KL, Davis BR, Baimbridge C, Ciocon JO, Cuyjet AB, Dart RA,...ALLHAT Collaborative Research Group. (2013 August). Long-term follow-up of moderately hypercholesterolemic hypertensive patients following randomization to pravastatin vs usual care: the Antihypertensive and Lipid-Lowering Treatment to Prevent Heart Attack Trial (ALLHAT-LLT). J Clin Hypertens (Greenwich). 15(8):542-54.
    PubMed ID: 23889716
  • Maenner M, Baker M, Broman KW, Tian J, Barnes J, Atkins A,...Mailick M [including McPherson EW, Brilliant MH.] (2013 July). FMR1 CGG expansions: Prevalence and sex ratios. Am J Med Genet B Neuropsychiatr Genet. 162(5):466-73.
    PubMed ID: 23740716
  • Pasquale L, Loomis S, Weinreb R, Kang J, Yaspan B, Bailey J,...Wiggs J [including Brilliant MH.] (2013 July). Estrogen pathway polymorphisms in relation to primary open angle glaucoma: an analysis accounting for gender from the United States. MOLECULAR VISION. 19 :1471-81.
    PubMed ID: 23869166
  • Martignetti JA, Tian L, Li D, Ramirez MC, Camacho-Vanegas O, Camacho SC,...Hakonarson H [including McPherson EW.] (2013 June 6). Mutations in PDGFRB cause autosomal-dominant infantile myofibromatosis. Am J Hum Genet. 92(6):1001-7.
    PubMed ID: 23731542
  • Newton KM, Peissig PL, Kho A, Bielinski S, Berg RL, Choudhary V,...Denny J. (2013 June). Validation of electronic medical record-based phenotyping algorithms: results and lessons learned from the eMERGE network. JOURNAL OF THE AMERICAN MEDICAL INFORMATICS ASSOCIATION. 20(e1):e147-54.
    PubMed ID: 23531748
  • McDavid A, Crane P, Newton KM, Crosslin D, McCormick W, Weston N,...Carlson C [including Rottscheit CM, Peissig PL, Stefanski EL.] (2013 June). Enhancing the power of genetic association studies through the use of silver standard cases derived from electronic medical records. PLoS One. 8(6):e63481.
    PubMed ID: 23762230
  • Vinitsky A, Zaleski CA, Sajjad SM, McPherson EW. (2013 May). Intestinal Ganglioneuromatosis: Unusual Presentation of Cowden Syndrome Resulting in Delayed Diagnosis. American Journal of Medical Genetics Part A. 161(5):1085-90.
    PubMed ID: 23512313
  • McPherson EW. (2013 April). Discovering the cause of stillbirth. CURRENT OPINION IN OBSTETRICS & GYNECOLOGY. 25(2):152-6.
    PubMed ID: 23354074
  • Hebbring S, Schrodi SJ, Ye Z, Zhou Z, Page D, Brilliant MH. (2013 April). A PheWAS approach in studying HLA-DRB1*1501 GENES AND IMMUNITY. 14(3):187-91.
    PubMed ID: 23392276